Explain what we mean by pre-oxidation and pre-reduction. Why is it important to be able to destroy the reagents used for these purposes?

Short Answer

Expert verified

Pre-oxidation is an increasement of the oxidation number and Pre-reduction is a decreasement of the oxidation number. The reagent needs to be destroyed so it doesn't interfere with analytes during the titration.

Step by step solution

01

Definition of Adjustment of analyte oxidation state.

  • Before titration, the oxidation state of the analyte may also want to be adjusted.

  • Pre-adjustment should be quantitative, and extra pre-adjustment reagent should be eliminated to keep away from interfering with the succeeding titration.

  • Peroxydisulfate, Silver (II) oxide, and sodium bismuthate are amazing oxidants that may be without problems removed following pre- oxidation.

02

Determine the pre-oxidation and pre-reduction

  • Adjustment of oxidation state before the titration is called pre-oxidation and pre-reduction.

  • Pre-oxidation is an increasement of the oxidation number, for example Mn2+to MnO4.

  • Pre-reduction is a decreasement of the oxidation number, for exampleFe3ιto Fe2ι.

  • The reagent needs to be destroyed so it doesn't interfere with analytes during the titration.

  • Reagents that are used for pre-oxidation and pre-reduction are usually destroyed by boiling.

03

Examples of Pre-oxidation and pre-reduction

Pre-oxidation:

Peroxydisulfate S2O32- requires Ag- as a catalyst.

S2O32+Ag+SO42+SO4+Ag2+

Excess reagent destroyed:

2S2O82+2H2Oboiling4SO42+O2+4H-

Pre-reduction:

Stannous chloride SnCI2will reduce Fe3ιtoF2ιin hot

Excess reductant is then destroyed:

Sn2+2HgCI2Sn4+HgCI2+2CI

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Most popular questions from this chapter

Primary-standard-grade arsenic(III) oxide (As4O6)is a useful (but carcinogenic) reagent for standardizing oxidants includingMnO4-andI3-. To standardize MnO4-,As4O6is dissolved in base and then titrated with localid="1655103723885" MnO4-in acid. A small amount of iodide (I-)or iodate (IO3-)catalyzes the reaction betweenH3AsO3andMnO42-.

As4O6+8OH-֏4HAsO32-+2H2OHAsO32-+2H+֏H3AsO35H3AsO3+2MnO4-+6H+5H2AsO4+2Mn2++3H2O

(a) A 3.214-g aliquot ofKMnO4(FM 158.034) was dissolved in 1.000Lof water, heated to cause any reactions with impurities to occur, cooled, and filtered. What is the theoretical molarity of this solution ifKMnO4were pure and if none was consumed by impurities?

(b) What mass of localid="1655105254654" As4O6(FM 395.68 ) would be just sufficient to react with25.00mLofKMnO4solution in part (a)?

(c) It was found that0.1468gofAs4O6required 29.985mLofKMnO4ofsolution for the faint color of unreacted MnO4-to appear. In a blank titration,0.03mLofMnO4-was required to produce enough color to be seen. Calculate the molarity of the permanganate solution.

Warning! The Surgeon General has determined that this problem is hazardous to your health. The oxidation numbers of CUand Biin high-temperature superconductors of the type Bi2Sr2(Ca0xYa2)Cu2Ox(which could contain Cu2+,Cu3+,Bi3+ and Bi3+) can be measured by the following procedure. In Experiment, the superconductor is dissolved in 1MHClcontaining excess 2mMCuCl2Bi5+(written as BiO3-) and Cu3+ consume Cu+ to make Cu2+:

BiO3+2Cu++4H+BiO++2Cu2++2H2OCu3++Cu+2Cu2+

The excess, unreactedCu4is then titrated by coulometry (described in Chapter). In Experiment , the superconductor is dissolved in1mMFeCl24H2Ocontaining excessBi5+. reacts with therole="math" localid="1668352055227" Fe2+ butCu3+ does not react withdata-custom-editor="chemistry" Fe2+41.

role="math" localid="1668352140519" BiO3+2Fe2++4H+BiO++2Fe3++2H2OCu3++12H2OCu2++14O2+H+

The excess, unreacted is then titrated by coulometry. The total oxidation number of is measured in Experiment, and the oxidation number ofis determined in Experiment. The difference gives the oxidation number of.

(a) In Experiment AA2, a sample of Bi2Sr2CaCu2O5(FM760.37+15.9994x)(containing no yttrium) weighing 102.3mg was dissolved in 100.0mLof 1MHCl containing 2.000mMCuCl. After reaction with the superconductor, coulometry detected 0.1085 mmolof unreactedCu+ in the solution. In Experiment B, 94.6 mgof superconductor were dissolved in 100.0mL. of 1MHCl containing1.000mMFeCl-4H2O. After reaction with the superconductor, coulometry detected 0.0577 mmolof unreacted. Find the average oxidation numbers of Biand Cuin the superconductor and the oxygen stoichiometry coefficient, x.

(b) Find the uncertainties in the oxidation numbers and x if the quantities in Experiment Aare102.3(±0.2)mgand0.1085(±0.0007)mmoland the quantities in Experiment Bare94.6(±0.2)me and0.0577(±0.0007)mmol. Assume negligible uncertainty in other quantities.

Consider the titration of 25.0mLof 0.100M Sn2+ by 0.0500 MT3+in 1MHCI, using Pt and saturated calomel electrodes to find the end point.

(a) Write a balanced titration reaction.

(b) Write two different half-reactions for the indicator electrode.

(c) Write two different Nernst equations for the cell voltage.

(d) Calculate E at the following volumes ofTl3+:1.00,2.50,4.90,5.00,5.10and 10.0 mL. Sketch the titration curve.

In which technique, iodimetry or iodometry, is starch indicator not added until just before the end point? Why?

Select indicators from Table 16-2 that would be suitable for finding the end point in Figure 16-3. What color changes would be observed?

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